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Arteriovenous malformations

Summary of 100 consecutive supratentorial cases

Dwight Parkinson and Gary Bachers

T he demonstration by Harvey 21 of the directional flow through arteries and veins, and then Malpighi's 45 description of capillaries, set the stage for the recognition by Hunter 29, 30 and Steindel 81 of the arteriovenous malformation (AVM). It remained for Holman 25 to discourage attempts to obliterate such a lesion in the extremities by occlusion of entering or leaving vessels; he emphasized the importance of obliterating the fistula. Simultaneous publications by both Dandy 12 and Cushing and Bailey 10 recognized that the solution depended on

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Robert M. Crowell, Umberto DeGirolami and William H. Sweet

R eported cases of arteriovenous malformation (AVM) of the central nervous system in association with a primary brain tumor are very rare; 1, 3, 10 only one case of AVM accompanying oligodendroglioma has been previously recorded. 1 We are now reporting a case of oligodendroglioma within an AVM. Case Report First Admission In June, 1971, this 17-year-old right-handed man suddenly felt pain “like an explosion” in the right eye which persisted for approximately 4 hours. Similar headaches recurred almost daily after the first episode. In early July

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Richard A. Roski, John H. Gardner and Robert F. Spetzler

W e are reporting an unusual occurrence of a cryptic arteriovenous malformation (AVM) situated completely within the optic tract and chiasm. Surgical removal of the AVM resulted in complete resolution of the patient's visual problems. Case Report This 37-year-old man was admitted to the University Hospitals complaining of blurred vision for the past 5 to 6 days. A similar episode had occurred 6 months prior to admission, and cleared over several days. Each episode was associated with mild headache. Examination . Physical examination was entirely within

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Familial arteriovenous malformations

Report of four cases in one family

Michael C. Boyd, Paul Steinbok and Donald W. Paty

F amilial arteriovenous malformation (AVM) of the central nervous system has been reported only seven times in the English literature; 1–3, 6–8, 12 two of these cases have been associated with hereditary telangiectasia. 3, 7 In addition, two cases reported in German have been referred to by Aberfeld and Rao. 1 We report a family in which four members of two generations are proven to have AVM's. Case Reports Case 1 This 18-year-old man with a 2-year history of episodic blurring of vision and dizziness experienced two generalized seizures on the day

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Omar M. Arnaout, Bradley A. Gross, Christopher S. Eddleman, Bernard R. Bendok, Christopher C. Getch and H. Hunt Batjer

authors report no conflict of interest concerning the materials or methods used in this study or the findings specified in this paper. References 1 Al-Shahi R , Warlow C : A systematic review of the frequency and prognosis of arteriovenous malformations of the brain in adults . Brain 124 : 1900 – 1926 , 2001 2 Batjer H , Samson D : Arteriovenous malformations of the posterior fossa: clinical presentation, diagnostic evaluation and surgical treatment . Neurosurg Rev 9 : 287 – 296 , 1986 3 Brown RD Jr , Wiebers DO , Forbes G , O

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Naoya Kuwayama, Akira Takaku, Michiharu Nishijima, Shunro Endo and Masato Hirao

D ural arteriovenous malformations (AVM's) occur most frequently related to the cavernous sinus (so-called “spontaneous carotid cavernous fistulas”) and lateral sinuses (transverse and sigmoid sinuses). Two cases with multiple dural AVM's involving the cavernous and the lateral sinuses are reported. Although a few cases with multiple dural AVM's emptying into the superior sagittal sinus (SSS) and the lateral sinus have been reported, involvement of both the cavernous sinus and the lateral sinus is extremely rare. It is of interest that in one of these patients

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Ossama Al-Mefty, John R. Jinkins and John L. Fox

D ural arteriovenous malformations (AVM's) in the region of the transverse sigmoid sinus, although rare, represent a well-defined entity from both clinical and angiographic aspects. 1, 7–9, 13, 14 The etiology and pathology of these anomalies remain controversial. 1, 7, 12–14, 24, 25 The clinical findings are determined by the volume, direction, and route of the venous drainage. The disease often progresses, leading to increasing neurological deficits, elevation of intracranial pressure, hydrocephalus, seizures, and hemorrhage. 2, 7, 8, 13, 24 Unilateral

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Intracranial arteriovenous malformations

Conservative and surgical treatment

Beniamino Guidetti and Alberto Delitala

A lthough much has been written on the treatment of intracranial arteriovenous malformations (AVM's), there is still doubt as to the real advantages of surgical as opposed to conservative treatment. 3–5, 7, 10, 17, 20–22 Our report concerns the late results of a series of 145 patients with intracranial AVM's treated either conservatively or surgically. Clinical Material Of our 145 patients, 95 received surgical and 50 conservative treatment. The great majority of these patients were followed up from 2 to 25 years; 15 were lost to follow-up review, but

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Neil A. Martin and Charles B. Wilson

A s a general rule, arteriovenous malformations (AVM's) do not encompass viable brain; the vessels are separated by gliotic neural parenchyma. 4 This anatomic feature of AVM's permits their removal without damage to the functional brain that surrounds the malformation. We describe the technique and results of surgical excision of AVM's from the medial occipital lobe — that region which includes the visual cortex. Medial occipital AVM's have distinct clinical and anatomic features. Vascular malformations in this location have a tendency to cause migrainous

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Charles J. Hodge Jr. and Robert B. King

V ascular malformations of the choroid plexus are an unusual cause of subarachnoid hemorrhage. This case serves to point out some of the clinical characteristics of arteriovenous malformations of the choroid plexus. Case Report A 22-year-old right-handed woman was transferred to State University Hospital following her second subarachnoid hemorrhage. She had been well until 2 years prior to admission when she experienced the first subarachnoid hemorrhage, characterized by headache, stiff neck, and confusion. Bilateral carotid angiography was normal. She